Package 0406-6408-60

Brand: lubiprostone

Generic: lubiprostone
NDC Package

Package Facts

Identity

Package NDC 0406-6408-60
Digits Only 0406640860
Product NDC 0406-6408
Product ID 0406-6408_47c44abf-bfc1-49c3-96e0-91a508327d5a
Description

60 CAPSULE, GELATIN COATED in 1 BOTTLE (0406-6408-60)

Marketing

Marketing Status
Marketed Since 2024-05-01
Brand lubiprostone
Generic lubiprostone
Sample Package No

Linked Drug Pages (1)

Lubiprostone ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "47c44abf-bfc1-49c3-96e0-91a508327d5a", "openfda": {"nui": ["N0000175573", "N0000175456"], "unii": ["7662KG2R6K"], "rxcui": ["616578", "794639"], "spl_set_id": ["cdf79a5a-6857-4a32-8c54-8c435d1a7535"], "pharm_class_epc": ["Chloride Channel Activator [EPC]"], "pharm_class_moa": ["Chloride Channel Activators [MoA]"], "manufacturer_name": ["SpecGx LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "60 CAPSULE, GELATIN COATED in 1 BOTTLE (0406-6408-60)", "package_ndc": "0406-6408-60", "marketing_start_date": "20240501"}], "brand_name": "Lubiprostone", "product_id": "0406-6408_47c44abf-bfc1-49c3-96e0-91a508327d5a", "dosage_form": "CAPSULE, GELATIN COATED", "pharm_class": ["Chloride Channel Activator [EPC]", "Chloride Channel Activators [MoA]"], "product_ndc": "0406-6408", "generic_name": "Lubiprostone", "labeler_name": "SpecGx LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lubiprostone", "active_ingredients": [{"name": "LUBIPROSTONE", "strength": "8 ug/1"}], "application_number": "NDA021908", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "20240501", "listing_expiration_date": "20261231"}